Direct-to-consumer genetic testing :: summary of a workshop /
"Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be...
Gespeichert in:
| Körperschaften: | , , , , |
|---|---|
| Weitere Verfasser: | , |
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Washington, D.C. :
National Academies Press,
©2011.
|
| Schriftenreihe: | Online access: NCBI NCBI Bookshelf.
|
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | "Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be headed; they also demonstrate the need for serious discussion about the regulatory environment, patient privacy, and other policy implications of direct-to-consumer (DTC) genetic testing. Rapid advances in genetic research already have begun to transform clinical practice and our understanding of disease progression. Existing research has revealed a genetic basis or component for numerous diseases, including Parkinson's disease, Alzheimer's disease, diabetes, heart disease, and several forms of cancer. The availability of the human genome sequence and the HapMap, plummeting costs of high-throughput screening, and increasingly sophisticated computational analyses have led to an explosion of discoveries of linkages between patterns of genetic variation and disease susceptibility. While this research is by no means a straight path toward better public health, improved knowledge of the genetic linkages has the potential to change fundamentally the way health professionals and public health practitioners approach the prevention and treatment of disease. Realizing this potential will require greater sophistication in the interpretation of genetic tests, new training for physicians and other diagnosticians, and new approaches to communicating findings to the public. As this rapidly growing field matures, all of these questions require attention from a variety of perspectives. To discuss some of the foregoing issues, several units of the National Academies held a workshop on August 31 and September 1, 2009, to bring together a still-developing community of professionals from a variety of relevant disciplines, to educate the public and policy-makers about this emerging field, and to identify issues for future study. The meeting featured several invited presentations and discussions on the many technical, legal, policy, and ethical questions that such DTC testing raises, including: (1) overview of the current state of knowledge and the future research trajectory; (2) shared genes and emerging issues in privacy; (3) the regulatory framework; and (4) education of the public and the medical community."--Publisher's description |
| Beschreibung: | 1 online resource (xii, 93 pages) |
| Bibliographie: | Includes bibliographical references. |
| ISBN: | 9780309162173 0309162173 |
Internformat
MARC
| LEADER | 00000cam a2200000 a 4500 | ||
|---|---|---|---|
| 001 | ZDB-4-EBA-ocn703255596 | ||
| 003 | OCoLC | ||
| 005 | 20241004212047.0 | ||
| 006 | m o d | ||
| 007 | cr cnu|||||||| | ||
| 008 | 110222s2011 dcu ob 100 0 eng d | ||
| 040 | |a N$T |b eng |e pn |c N$T |d NRC |d E7B |d OCLCA |d BUF |d OCLCQ |d ZMC |d OCLCQ |d COO |d OCLCQ |d YDXCP |d OCLCA |d OCLCF |d OCLCQ |d NLGGC |d OCL |d OCLCQ |d EBLCP |d OCLCQ |d TOA |d ZCU |d MERUC |d OCLCQ |d OCLCO |d OCLCA |d VT2 |d OCLCO |d MERER |d OCLCO |d VNS |d VTS |d AGLDB |d ICG |d REC |d OCLCQ |d OCLCO |d WYU |d LVT |d STF |d DKC |d OCLCQ |d M8D |d UKAHL |d OCLCQ |d OCLCO |d SFB |d OCLCQ |d OCL |d INARC |d OCLCO |d OCLCL |d OCLCQ | ||
| 019 | |a 701715437 |a 923282752 |a 1028773966 |a 1229413951 | ||
| 020 | |a 9780309162173 |q (electronic bk.) | ||
| 020 | |a 0309162173 |q (electronic bk.) | ||
| 020 | |z 9780309162166 | ||
| 020 | |z 0309162165 | ||
| 035 | |a (OCoLC)703255596 |z (OCoLC)701715437 |z (OCoLC)923282752 |z (OCoLC)1028773966 |z (OCoLC)1229413951 | ||
| 050 | 4 | |a RB155.65 |b .I57 2011eb | |
| 060 | 4 | |a 2011 F-678 | |
| 060 | 4 | |a QZ 52 | |
| 072 | 7 | |a HEA |x 039060 |2 bisacsh | |
| 072 | 7 | |a MED |x 107000 |2 bisacsh | |
| 082 | 7 | |a 616.042 |2 22 | |
| 049 | |a MAIN | ||
| 110 | 2 | |a National Research Council (U.S.). |b Committee on Science, Technology, and Law. |0 http://id.loc.gov/authorities/names/n2006032073 | |
| 245 | 1 | 0 | |a Direct-to-consumer genetic testing : |b summary of a workshop / |c Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies. |
| 260 | |a Washington, D.C. : |b National Academies Press, |c ©2011. | ||
| 300 | |a 1 online resource (xii, 93 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references. | ||
| 505 | 0 | 0 | |t Introduction -- |t Scientific foundations for direct-to-consumer genetic testing -- |t Personal and social issues -- |t Research and medical issues -- |t Impact on health care and public health -- |t Current legislative and regulatory framework in the United States -- |t Areas for further study. |
| 520 | |a "Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be headed; they also demonstrate the need for serious discussion about the regulatory environment, patient privacy, and other policy implications of direct-to-consumer (DTC) genetic testing. Rapid advances in genetic research already have begun to transform clinical practice and our understanding of disease progression. Existing research has revealed a genetic basis or component for numerous diseases, including Parkinson's disease, Alzheimer's disease, diabetes, heart disease, and several forms of cancer. The availability of the human genome sequence and the HapMap, plummeting costs of high-throughput screening, and increasingly sophisticated computational analyses have led to an explosion of discoveries of linkages between patterns of genetic variation and disease susceptibility. While this research is by no means a straight path toward better public health, improved knowledge of the genetic linkages has the potential to change fundamentally the way health professionals and public health practitioners approach the prevention and treatment of disease. Realizing this potential will require greater sophistication in the interpretation of genetic tests, new training for physicians and other diagnosticians, and new approaches to communicating findings to the public. As this rapidly growing field matures, all of these questions require attention from a variety of perspectives. To discuss some of the foregoing issues, several units of the National Academies held a workshop on August 31 and September 1, 2009, to bring together a still-developing community of professionals from a variety of relevant disciplines, to educate the public and policy-makers about this emerging field, and to identify issues for future study. The meeting featured several invited presentations and discussions on the many technical, legal, policy, and ethical questions that such DTC testing raises, including: (1) overview of the current state of knowledge and the future research trajectory; (2) shared genes and emerging issues in privacy; (3) the regulatory framework; and (4) education of the public and the medical community."--Publisher's description | ||
| 588 | 0 | |a Print version record. | |
| 650 | 0 | |a Human chromosome abnormalities |x Diagnosis |v Congresses. | |
| 650 | 0 | |a Self-examination, Medical |v Congresses. | |
| 650 | 0 | |a Genetic screening. |0 http://id.loc.gov/authorities/subjects/sh99000370 | |
| 650 | 0 | |a Self-care, Health. |0 http://id.loc.gov/authorities/subjects/sh85119714 | |
| 650 | 1 | 2 | |a Genetic Testing |0 https://id.nlm.nih.gov/mesh/D005820 |
| 650 | 2 | 2 | |a Genetic Predisposition to Disease |0 https://id.nlm.nih.gov/mesh/D020022 |
| 650 | 2 | 2 | |a Marketing of Health Services |0 https://id.nlm.nih.gov/mesh/D008389 |
| 650 | 2 | 2 | |a Self Care |0 https://id.nlm.nih.gov/mesh/D012648 |
| 650 | 6 | |a Chromosomes humains |x Anomalies |x Diagnostic |v Congrès. | |
| 650 | 6 | |a Auto-examen médical |v Congrès. | |
| 650 | 6 | |a Dépistage génétique. | |
| 650 | 6 | |a Autothérapie. | |
| 650 | 7 | |a HEALTH & FITNESS |x Diseases |x Genetic. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Genetics. |2 bisacsh | |
| 650 | 7 | |a Self-care, Health |2 fast | |
| 650 | 7 | |a Genetic screening |2 fast | |
| 650 | 7 | |a Human chromosome abnormalities |x Diagnosis |2 fast | |
| 650 | 7 | |a Self-examination, Medical |2 fast | |
| 655 | 2 | |a Congress |0 https://id.nlm.nih.gov/mesh/D016423 | |
| 655 | 7 | |a proceedings (reports) |2 aat | |
| 655 | 7 | |a Conference papers and proceedings |2 fast | |
| 655 | 7 | |a Conference papers and proceedings. |2 lcgft |0 http://id.loc.gov/authorities/genreForms/gf2014026068 | |
| 655 | 7 | |a Actes de congrès. |2 rvmgf | |
| 700 | 1 | |a Fraker, Mary. |0 http://id.loc.gov/authorities/names/n97869895 | |
| 700 | 1 | |a Mazza, Anne-Marie. |0 http://id.loc.gov/authorities/names/no2006037335 | |
| 710 | 2 | |a National Research Council (U.S.). |b Board on Life Sciences. |0 http://id.loc.gov/authorities/names/no2001073517 | |
| 710 | 2 | |a Institute of Medicine (U.S.). |b Forum on Drug Discovery, Development, and Translation. |0 http://id.loc.gov/authorities/names/no2007051854 | |
| 710 | 2 | |a Institute of Medicine (U.S.). |b Roundtable on Translating Genomic-Based Research for Health. |0 http://id.loc.gov/authorities/names/no2008119550 | |
| 710 | 2 | |a National Cancer Policy Forum (U.S.) |0 http://id.loc.gov/authorities/names/n2006183479 | |
| 776 | 0 | 8 | |i Print version: |a National Research Council (U.S.). Committee on Science, Technology, and Law Policy and Global Affairs. |t Direct-to-consumer genetic testing. |d Washington, D.C. : National Academies Press, ©2011 |z 9780309162166 |w (OCoLC)698376202 |
| 830 | 0 | |a Online access: NCBI NCBI Bookshelf. | |
| 856 | 4 | 0 | |l FWS01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350899 |3 Volltext |
| 938 | |a Internet Archive |b INAR |n directtoconsumer0000nati | ||
| 938 | |a Askews and Holts Library Services |b ASKH |n AH36617293 | ||
| 938 | |a Askews and Holts Library Services |b ASKH |n AH36559510 | ||
| 938 | |a ProQuest Ebook Central |b EBLB |n EBL3378712 | ||
| 938 | |a ebrary |b EBRY |n ebr10439392 | ||
| 938 | |a EBSCOhost |b EBSC |n 350899 | ||
| 938 | |a YBP Library Services |b YANK |n 3636003 | ||
| 994 | |a 92 |b GEBAY | ||
| 912 | |a ZDB-4-EBA | ||
| 049 | |a DE-863 | ||
Datensatz im Suchindex
| DE-BY-FWS_katkey | ZDB-4-EBA-ocn703255596 |
|---|---|
| _version_ | 1816881751877746689 |
| adam_text | |
| any_adam_object | |
| author2 | Fraker, Mary Mazza, Anne-Marie |
| author2_role | |
| author2_variant | m f mf a m m amm |
| author_GND | http://id.loc.gov/authorities/names/n97869895 http://id.loc.gov/authorities/names/no2006037335 |
| author_corporate | National Research Council (U.S.). Committee on Science, Technology, and Law National Research Council (U.S.). Board on Life Sciences Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health National Cancer Policy Forum (U.S.) |
| author_corporate_role | |
| author_facet | Fraker, Mary Mazza, Anne-Marie National Research Council (U.S.). Committee on Science, Technology, and Law National Research Council (U.S.). Board on Life Sciences Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health National Cancer Policy Forum (U.S.) |
| author_sort | National Research Council (U.S.). Committee on Science, Technology, and Law |
| building | Verbundindex |
| bvnumber | localFWS |
| callnumber-first | R - Medicine |
| callnumber-label | RB155 |
| callnumber-raw | RB155.65 .I57 2011eb |
| callnumber-search | RB155.65 .I57 2011eb |
| callnumber-sort | RB 3155.65 I57 42011EB |
| callnumber-subject | RB - Pathology |
| collection | ZDB-4-EBA |
| contents | Introduction -- Scientific foundations for direct-to-consumer genetic testing -- Personal and social issues -- Research and medical issues -- Impact on health care and public health -- Current legislative and regulatory framework in the United States -- Areas for further study. |
| ctrlnum | (OCoLC)703255596 |
| dewey-full | 616.042 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 616 - Diseases |
| dewey-raw | 616.042 |
| dewey-search | 616.042 |
| dewey-sort | 3616.042 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>07578cam a2200877 a 4500</leader><controlfield tag="001">ZDB-4-EBA-ocn703255596</controlfield><controlfield tag="003">OCoLC</controlfield><controlfield tag="005">20241004212047.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr cnu||||||||</controlfield><controlfield tag="008">110222s2011 dcu ob 100 0 eng d</controlfield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">N$T</subfield><subfield code="b">eng</subfield><subfield code="e">pn</subfield><subfield code="c">N$T</subfield><subfield code="d">NRC</subfield><subfield code="d">E7B</subfield><subfield code="d">OCLCA</subfield><subfield code="d">BUF</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">ZMC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">COO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">YDXCP</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCF</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">NLGGC</subfield><subfield code="d">OCL</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">EBLCP</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">TOA</subfield><subfield code="d">ZCU</subfield><subfield code="d">MERUC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">VT2</subfield><subfield code="d">OCLCO</subfield><subfield code="d">MERER</subfield><subfield code="d">OCLCO</subfield><subfield code="d">VNS</subfield><subfield code="d">VTS</subfield><subfield code="d">AGLDB</subfield><subfield code="d">ICG</subfield><subfield code="d">REC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">WYU</subfield><subfield code="d">LVT</subfield><subfield code="d">STF</subfield><subfield code="d">DKC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">M8D</subfield><subfield code="d">UKAHL</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">SFB</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCL</subfield><subfield code="d">INARC</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCL</subfield><subfield code="d">OCLCQ</subfield></datafield><datafield tag="019" ind1=" " ind2=" "><subfield code="a">701715437</subfield><subfield code="a">923282752</subfield><subfield code="a">1028773966</subfield><subfield code="a">1229413951</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780309162173</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0309162173</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="z">9780309162166</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="z">0309162165</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)703255596</subfield><subfield code="z">(OCoLC)701715437</subfield><subfield code="z">(OCoLC)923282752</subfield><subfield code="z">(OCoLC)1028773966</subfield><subfield code="z">(OCoLC)1229413951</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">RB155.65</subfield><subfield code="b">.I57 2011eb</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">2011 F-678</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">QZ 52</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">HEA</subfield><subfield code="x">039060</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">MED</subfield><subfield code="x">107000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="082" ind1="7" ind2=" "><subfield code="a">616.042</subfield><subfield code="2">22</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">MAIN</subfield></datafield><datafield tag="110" ind1="2" ind2=" "><subfield code="a">National Research Council (U.S.).</subfield><subfield code="b">Committee on Science, Technology, and Law.</subfield><subfield code="0">http://id.loc.gov/authorities/names/n2006032073</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Direct-to-consumer genetic testing :</subfield><subfield code="b">summary of a workshop /</subfield><subfield code="c">Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Washington, D.C. :</subfield><subfield code="b">National Academies Press,</subfield><subfield code="c">©2011.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xii, 93 pages)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references.</subfield></datafield><datafield tag="505" ind1="0" ind2="0"><subfield code="t">Introduction --</subfield><subfield code="t">Scientific foundations for direct-to-consumer genetic testing --</subfield><subfield code="t">Personal and social issues --</subfield><subfield code="t">Research and medical issues --</subfield><subfield code="t">Impact on health care and public health --</subfield><subfield code="t">Current legislative and regulatory framework in the United States --</subfield><subfield code="t">Areas for further study.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">"Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be headed; they also demonstrate the need for serious discussion about the regulatory environment, patient privacy, and other policy implications of direct-to-consumer (DTC) genetic testing. Rapid advances in genetic research already have begun to transform clinical practice and our understanding of disease progression. Existing research has revealed a genetic basis or component for numerous diseases, including Parkinson's disease, Alzheimer's disease, diabetes, heart disease, and several forms of cancer. The availability of the human genome sequence and the HapMap, plummeting costs of high-throughput screening, and increasingly sophisticated computational analyses have led to an explosion of discoveries of linkages between patterns of genetic variation and disease susceptibility. While this research is by no means a straight path toward better public health, improved knowledge of the genetic linkages has the potential to change fundamentally the way health professionals and public health practitioners approach the prevention and treatment of disease. Realizing this potential will require greater sophistication in the interpretation of genetic tests, new training for physicians and other diagnosticians, and new approaches to communicating findings to the public. As this rapidly growing field matures, all of these questions require attention from a variety of perspectives. To discuss some of the foregoing issues, several units of the National Academies held a workshop on August 31 and September 1, 2009, to bring together a still-developing community of professionals from a variety of relevant disciplines, to educate the public and policy-makers about this emerging field, and to identify issues for future study. The meeting featured several invited presentations and discussions on the many technical, legal, policy, and ethical questions that such DTC testing raises, including: (1) overview of the current state of knowledge and the future research trajectory; (2) shared genes and emerging issues in privacy; (3) the regulatory framework; and (4) education of the public and the medical community."--Publisher's description</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Print version record.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="x">Diagnosis</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Self-examination, Medical</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetic screening.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh99000370</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Self-care, Health.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85119714</subfield></datafield><datafield tag="650" ind1="1" ind2="2"><subfield code="a">Genetic Testing</subfield><subfield code="0">https://id.nlm.nih.gov/mesh/D005820</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Genetic Predisposition to Disease</subfield><subfield code="0">https://id.nlm.nih.gov/mesh/D020022</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Marketing of Health Services</subfield><subfield code="0">https://id.nlm.nih.gov/mesh/D008389</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Self Care</subfield><subfield code="0">https://id.nlm.nih.gov/mesh/D012648</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Chromosomes humains</subfield><subfield code="x">Anomalies</subfield><subfield code="x">Diagnostic</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Auto-examen médical</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Dépistage génétique.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Autothérapie.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">HEALTH & FITNESS</subfield><subfield code="x">Diseases</subfield><subfield code="x">Genetic.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">MEDICAL</subfield><subfield code="x">Genetics.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Self-care, Health</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetic screening</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="x">Diagnosis</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Self-examination, Medical</subfield><subfield code="2">fast</subfield></datafield><datafield tag="655" ind1=" " ind2="2"><subfield code="a">Congress</subfield><subfield code="0">https://id.nlm.nih.gov/mesh/D016423</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="a">proceedings (reports)</subfield><subfield code="2">aat</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="a">Conference papers and proceedings</subfield><subfield code="2">fast</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="a">Conference papers and proceedings.</subfield><subfield code="2">lcgft</subfield><subfield code="0">http://id.loc.gov/authorities/genreForms/gf2014026068</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="a">Actes de congrès.</subfield><subfield code="2">rvmgf</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Fraker, Mary.</subfield><subfield code="0">http://id.loc.gov/authorities/names/n97869895</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mazza, Anne-Marie.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2006037335</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">National Research Council (U.S.).</subfield><subfield code="b">Board on Life Sciences.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2001073517</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">Institute of Medicine (U.S.).</subfield><subfield code="b">Forum on Drug Discovery, Development, and Translation.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2007051854</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">Institute of Medicine (U.S.).</subfield><subfield code="b">Roundtable on Translating Genomic-Based Research for Health.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2008119550</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">National Cancer Policy Forum (U.S.)</subfield><subfield code="0">http://id.loc.gov/authorities/names/n2006183479</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Print version:</subfield><subfield code="a">National Research Council (U.S.). Committee on Science, Technology, and Law Policy and Global Affairs.</subfield><subfield code="t">Direct-to-consumer genetic testing.</subfield><subfield code="d">Washington, D.C. : National Academies Press, ©2011</subfield><subfield code="z">9780309162166</subfield><subfield code="w">(OCoLC)698376202</subfield></datafield><datafield tag="830" ind1=" " ind2="0"><subfield code="a">Online access: NCBI NCBI Bookshelf.</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="l">FWS01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FWS_PDA_EBA</subfield><subfield code="u">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350899</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Internet Archive</subfield><subfield code="b">INAR</subfield><subfield code="n">directtoconsumer0000nati</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Askews and Holts Library Services</subfield><subfield code="b">ASKH</subfield><subfield code="n">AH36617293</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Askews and Holts Library Services</subfield><subfield code="b">ASKH</subfield><subfield code="n">AH36559510</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ProQuest Ebook Central</subfield><subfield code="b">EBLB</subfield><subfield code="n">EBL3378712</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ebrary</subfield><subfield code="b">EBRY</subfield><subfield code="n">ebr10439392</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">EBSCOhost</subfield><subfield code="b">EBSC</subfield><subfield code="n">350899</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">3636003</subfield></datafield><datafield tag="994" ind1=" " ind2=" "><subfield code="a">92</subfield><subfield code="b">GEBAY</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-EBA</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-863</subfield></datafield></record></collection> |
| genre | Congress https://id.nlm.nih.gov/mesh/D016423 proceedings (reports) aat Conference papers and proceedings fast Conference papers and proceedings. lcgft http://id.loc.gov/authorities/genreForms/gf2014026068 Actes de congrès. rvmgf |
| genre_facet | Congress proceedings (reports) Conference papers and proceedings Conference papers and proceedings. Actes de congrès. |
| id | ZDB-4-EBA-ocn703255596 |
| illustrated | Not Illustrated |
| indexdate | 2024-11-27T13:17:42Z |
| institution | BVB |
| institution_GND | http://id.loc.gov/authorities/names/n2006032073 http://id.loc.gov/authorities/names/no2001073517 http://id.loc.gov/authorities/names/no2007051854 http://id.loc.gov/authorities/names/no2008119550 http://id.loc.gov/authorities/names/n2006183479 |
| isbn | 9780309162173 0309162173 |
| language | English |
| oclc_num | 703255596 |
| open_access_boolean | |
| owner | MAIN DE-863 DE-BY-FWS |
| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xii, 93 pages) |
| psigel | ZDB-4-EBA |
| publishDate | 2011 |
| publishDateSearch | 2011 |
| publishDateSort | 2011 |
| publisher | National Academies Press, |
| record_format | marc |
| series | Online access: NCBI NCBI Bookshelf. |
| spelling | National Research Council (U.S.). Committee on Science, Technology, and Law. http://id.loc.gov/authorities/names/n2006032073 Direct-to-consumer genetic testing : summary of a workshop / Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies. Washington, D.C. : National Academies Press, ©2011. 1 online resource (xii, 93 pages) text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references. Introduction -- Scientific foundations for direct-to-consumer genetic testing -- Personal and social issues -- Research and medical issues -- Impact on health care and public health -- Current legislative and regulatory framework in the United States -- Areas for further study. "Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be headed; they also demonstrate the need for serious discussion about the regulatory environment, patient privacy, and other policy implications of direct-to-consumer (DTC) genetic testing. Rapid advances in genetic research already have begun to transform clinical practice and our understanding of disease progression. Existing research has revealed a genetic basis or component for numerous diseases, including Parkinson's disease, Alzheimer's disease, diabetes, heart disease, and several forms of cancer. The availability of the human genome sequence and the HapMap, plummeting costs of high-throughput screening, and increasingly sophisticated computational analyses have led to an explosion of discoveries of linkages between patterns of genetic variation and disease susceptibility. While this research is by no means a straight path toward better public health, improved knowledge of the genetic linkages has the potential to change fundamentally the way health professionals and public health practitioners approach the prevention and treatment of disease. Realizing this potential will require greater sophistication in the interpretation of genetic tests, new training for physicians and other diagnosticians, and new approaches to communicating findings to the public. As this rapidly growing field matures, all of these questions require attention from a variety of perspectives. To discuss some of the foregoing issues, several units of the National Academies held a workshop on August 31 and September 1, 2009, to bring together a still-developing community of professionals from a variety of relevant disciplines, to educate the public and policy-makers about this emerging field, and to identify issues for future study. The meeting featured several invited presentations and discussions on the many technical, legal, policy, and ethical questions that such DTC testing raises, including: (1) overview of the current state of knowledge and the future research trajectory; (2) shared genes and emerging issues in privacy; (3) the regulatory framework; and (4) education of the public and the medical community."--Publisher's description Print version record. Human chromosome abnormalities Diagnosis Congresses. Self-examination, Medical Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Self-care, Health. http://id.loc.gov/authorities/subjects/sh85119714 Genetic Testing https://id.nlm.nih.gov/mesh/D005820 Genetic Predisposition to Disease https://id.nlm.nih.gov/mesh/D020022 Marketing of Health Services https://id.nlm.nih.gov/mesh/D008389 Self Care https://id.nlm.nih.gov/mesh/D012648 Chromosomes humains Anomalies Diagnostic Congrès. Auto-examen médical Congrès. Dépistage génétique. Autothérapie. HEALTH & FITNESS Diseases Genetic. bisacsh MEDICAL Genetics. bisacsh Self-care, Health fast Genetic screening fast Human chromosome abnormalities Diagnosis fast Self-examination, Medical fast Congress https://id.nlm.nih.gov/mesh/D016423 proceedings (reports) aat Conference papers and proceedings fast Conference papers and proceedings. lcgft http://id.loc.gov/authorities/genreForms/gf2014026068 Actes de congrès. rvmgf Fraker, Mary. http://id.loc.gov/authorities/names/n97869895 Mazza, Anne-Marie. http://id.loc.gov/authorities/names/no2006037335 National Research Council (U.S.). Board on Life Sciences. http://id.loc.gov/authorities/names/no2001073517 Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation. http://id.loc.gov/authorities/names/no2007051854 Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health. http://id.loc.gov/authorities/names/no2008119550 National Cancer Policy Forum (U.S.) http://id.loc.gov/authorities/names/n2006183479 Print version: National Research Council (U.S.). Committee on Science, Technology, and Law Policy and Global Affairs. Direct-to-consumer genetic testing. Washington, D.C. : National Academies Press, ©2011 9780309162166 (OCoLC)698376202 Online access: NCBI NCBI Bookshelf. FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350899 Volltext |
| spellingShingle | Direct-to-consumer genetic testing : summary of a workshop / Online access: NCBI NCBI Bookshelf. Introduction -- Scientific foundations for direct-to-consumer genetic testing -- Personal and social issues -- Research and medical issues -- Impact on health care and public health -- Current legislative and regulatory framework in the United States -- Areas for further study. Human chromosome abnormalities Diagnosis Congresses. Self-examination, Medical Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Self-care, Health. http://id.loc.gov/authorities/subjects/sh85119714 Genetic Testing https://id.nlm.nih.gov/mesh/D005820 Genetic Predisposition to Disease https://id.nlm.nih.gov/mesh/D020022 Marketing of Health Services https://id.nlm.nih.gov/mesh/D008389 Self Care https://id.nlm.nih.gov/mesh/D012648 Chromosomes humains Anomalies Diagnostic Congrès. Auto-examen médical Congrès. Dépistage génétique. Autothérapie. HEALTH & FITNESS Diseases Genetic. bisacsh MEDICAL Genetics. bisacsh Self-care, Health fast Genetic screening fast Human chromosome abnormalities Diagnosis fast Self-examination, Medical fast |
| subject_GND | http://id.loc.gov/authorities/subjects/sh99000370 http://id.loc.gov/authorities/subjects/sh85119714 https://id.nlm.nih.gov/mesh/D005820 https://id.nlm.nih.gov/mesh/D020022 https://id.nlm.nih.gov/mesh/D008389 https://id.nlm.nih.gov/mesh/D012648 https://id.nlm.nih.gov/mesh/D016423 http://id.loc.gov/authorities/genreForms/gf2014026068 |
| title | Direct-to-consumer genetic testing : summary of a workshop / |
| title_alt | Introduction -- Scientific foundations for direct-to-consumer genetic testing -- Personal and social issues -- Research and medical issues -- Impact on health care and public health -- Current legislative and regulatory framework in the United States -- Areas for further study. |
| title_auth | Direct-to-consumer genetic testing : summary of a workshop / |
| title_exact_search | Direct-to-consumer genetic testing : summary of a workshop / |
| title_full | Direct-to-consumer genetic testing : summary of a workshop / Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies. |
| title_fullStr | Direct-to-consumer genetic testing : summary of a workshop / Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies. |
| title_full_unstemmed | Direct-to-consumer genetic testing : summary of a workshop / Mary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs, Board on Life Sciences [and others], Institute of Medicine and National Research Council of the National Academies. |
| title_short | Direct-to-consumer genetic testing : |
| title_sort | direct to consumer genetic testing summary of a workshop |
| title_sub | summary of a workshop / |
| topic | Human chromosome abnormalities Diagnosis Congresses. Self-examination, Medical Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Self-care, Health. http://id.loc.gov/authorities/subjects/sh85119714 Genetic Testing https://id.nlm.nih.gov/mesh/D005820 Genetic Predisposition to Disease https://id.nlm.nih.gov/mesh/D020022 Marketing of Health Services https://id.nlm.nih.gov/mesh/D008389 Self Care https://id.nlm.nih.gov/mesh/D012648 Chromosomes humains Anomalies Diagnostic Congrès. Auto-examen médical Congrès. Dépistage génétique. Autothérapie. HEALTH & FITNESS Diseases Genetic. bisacsh MEDICAL Genetics. bisacsh Self-care, Health fast Genetic screening fast Human chromosome abnormalities Diagnosis fast Self-examination, Medical fast |
| topic_facet | Human chromosome abnormalities Diagnosis Congresses. Self-examination, Medical Congresses. Genetic screening. Self-care, Health. Genetic Testing Genetic Predisposition to Disease Marketing of Health Services Self Care Chromosomes humains Anomalies Diagnostic Congrès. Auto-examen médical Congrès. Dépistage génétique. Autothérapie. HEALTH & FITNESS Diseases Genetic. MEDICAL Genetics. Self-care, Health Genetic screening Human chromosome abnormalities Diagnosis Self-examination, Medical Congress proceedings (reports) Conference papers and proceedings Conference papers and proceedings. Actes de congrès. |
| url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350899 |
| work_keys_str_mv | AT nationalresearchcounciluscommitteeonsciencetechnologyandlaw directtoconsumergenetictestingsummaryofaworkshop AT frakermary directtoconsumergenetictestingsummaryofaworkshop AT mazzaannemarie directtoconsumergenetictestingsummaryofaworkshop AT nationalresearchcouncilusboardonlifesciences directtoconsumergenetictestingsummaryofaworkshop AT instituteofmedicineusforumondrugdiscoverydevelopmentandtranslation directtoconsumergenetictestingsummaryofaworkshop AT instituteofmedicineusroundtableontranslatinggenomicbasedresearchforhealth directtoconsumergenetictestingsummaryofaworkshop AT nationalcancerpolicyforumus directtoconsumergenetictestingsummaryofaworkshop |